Cargando…

IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses

Type I Interferons (IFN-I) are important inducers of the antiviral immune response and immune modulators. IFN-β is the most highly expressed IFN-I in the central nervous system (CNS). The infection of SJL mice with the BeAn or the DA strain of Theiler’s murine encephalomyelitis virus (TMEV) results...

Descripción completa

Detalles Bibliográficos
Autores principales: Bühler, Melanie, Runft, Sandra, Li, Dandan, Götting, Jasper, Detje, Claudia N., Nippold, Vanessa, Stoff, Melanie, Beineke, Andreas, Schulz, Thomas, Kalinke, Ulrich, Baumgärtner, Wolfgang, Gerhauser, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864290/
https://www.ncbi.nlm.nih.gov/pubmed/35222374
http://dx.doi.org/10.3389/fimmu.2022.786940
_version_ 1784655431169212416
author Bühler, Melanie
Runft, Sandra
Li, Dandan
Götting, Jasper
Detje, Claudia N.
Nippold, Vanessa
Stoff, Melanie
Beineke, Andreas
Schulz, Thomas
Kalinke, Ulrich
Baumgärtner, Wolfgang
Gerhauser, Ingo
author_facet Bühler, Melanie
Runft, Sandra
Li, Dandan
Götting, Jasper
Detje, Claudia N.
Nippold, Vanessa
Stoff, Melanie
Beineke, Andreas
Schulz, Thomas
Kalinke, Ulrich
Baumgärtner, Wolfgang
Gerhauser, Ingo
author_sort Bühler, Melanie
collection PubMed
description Type I Interferons (IFN-I) are important inducers of the antiviral immune response and immune modulators. IFN-β is the most highly expressed IFN-I in the central nervous system (CNS). The infection of SJL mice with the BeAn or the DA strain of Theiler’s murine encephalomyelitis virus (TMEV) results in a progressive demyelinating disease. C57BL/6 mice are usually resistant to TMEV-induced demyelination and eliminate these strains from the CNS within several weeks. Using C57BL/6 IFN-β knockout (IFN-β(-/-)) mice infected with TMEV, we evaluated the role of IFN-β in neuroinfection. Despite the resistance of C57BL/6 wild type (WT) mice to TMEV infection, DA-infected IFN-β(-/-) mice had to be killed at 7 to 8 days post infection (dpi) due to severe clinical disease. In contrast, BeAn-infected IFN-β(-/-) mice survived until 98 dpi. Nevertheless at 14 dpi, BeAn-infected IFN-β(-/-) mice showed a stronger encephalitis and astrogliosis, higher viral load as well as higher mRNA levels of Isg15, Eif2ak2 (PKR), Tnfa, Il1b, Il10, Il12 and Ifng in the cerebrum than BeAn-infected WT mice. Moreover, the majority of IFN-β(-/-) mice did not clear the virus from the CNS and developed mild demyelination in the spinal cord at 98 dpi, whereas virus and lesions were absent in the spinal cord of WT mice. Persistently infected IFN-β(-/-) mice also had higher Isg15, Eif2ak1, Tnfa, Il1a, Il1b and Ifng mRNA levels in the spinal cord at 98 dpi than their virus-negative counterparts indicating an activation of IFN-I signaling and ongoing inflammation. Most importantly, BeAn-infected NesCre(+/-) IFN-β(fl/fl) mice, which do not express IFN-β in neurons, astrocytes and oligodendrocytes, only developed mild brain lesions similar to WT mice. Consequently, IFN-β produced by neuroectodermal cells does not seem to play a critical role in the resistance of C57BL/6 mice against fatal and demyelinating disease induced by TMEV strains.
format Online
Article
Text
id pubmed-8864290
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-88642902022-02-24 IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses Bühler, Melanie Runft, Sandra Li, Dandan Götting, Jasper Detje, Claudia N. Nippold, Vanessa Stoff, Melanie Beineke, Andreas Schulz, Thomas Kalinke, Ulrich Baumgärtner, Wolfgang Gerhauser, Ingo Front Immunol Immunology Type I Interferons (IFN-I) are important inducers of the antiviral immune response and immune modulators. IFN-β is the most highly expressed IFN-I in the central nervous system (CNS). The infection of SJL mice with the BeAn or the DA strain of Theiler’s murine encephalomyelitis virus (TMEV) results in a progressive demyelinating disease. C57BL/6 mice are usually resistant to TMEV-induced demyelination and eliminate these strains from the CNS within several weeks. Using C57BL/6 IFN-β knockout (IFN-β(-/-)) mice infected with TMEV, we evaluated the role of IFN-β in neuroinfection. Despite the resistance of C57BL/6 wild type (WT) mice to TMEV infection, DA-infected IFN-β(-/-) mice had to be killed at 7 to 8 days post infection (dpi) due to severe clinical disease. In contrast, BeAn-infected IFN-β(-/-) mice survived until 98 dpi. Nevertheless at 14 dpi, BeAn-infected IFN-β(-/-) mice showed a stronger encephalitis and astrogliosis, higher viral load as well as higher mRNA levels of Isg15, Eif2ak2 (PKR), Tnfa, Il1b, Il10, Il12 and Ifng in the cerebrum than BeAn-infected WT mice. Moreover, the majority of IFN-β(-/-) mice did not clear the virus from the CNS and developed mild demyelination in the spinal cord at 98 dpi, whereas virus and lesions were absent in the spinal cord of WT mice. Persistently infected IFN-β(-/-) mice also had higher Isg15, Eif2ak1, Tnfa, Il1a, Il1b and Ifng mRNA levels in the spinal cord at 98 dpi than their virus-negative counterparts indicating an activation of IFN-I signaling and ongoing inflammation. Most importantly, BeAn-infected NesCre(+/-) IFN-β(fl/fl) mice, which do not express IFN-β in neurons, astrocytes and oligodendrocytes, only developed mild brain lesions similar to WT mice. Consequently, IFN-β produced by neuroectodermal cells does not seem to play a critical role in the resistance of C57BL/6 mice against fatal and demyelinating disease induced by TMEV strains. Frontiers Media S.A. 2022-02-09 /pmc/articles/PMC8864290/ /pubmed/35222374 http://dx.doi.org/10.3389/fimmu.2022.786940 Text en Copyright © 2022 Bühler, Runft, Li, Götting, Detje, Nippold, Stoff, Beineke, Schulz, Kalinke, Baumgärtner and Gerhauser https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bühler, Melanie
Runft, Sandra
Li, Dandan
Götting, Jasper
Detje, Claudia N.
Nippold, Vanessa
Stoff, Melanie
Beineke, Andreas
Schulz, Thomas
Kalinke, Ulrich
Baumgärtner, Wolfgang
Gerhauser, Ingo
IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses
title IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses
title_full IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses
title_fullStr IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses
title_full_unstemmed IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses
title_short IFN-β Deficiency Results in Fatal or Demyelinating Disease in C57BL/6 Mice Infected With Theiler’s Murine Encephalomyelitis Viruses
title_sort ifn-β deficiency results in fatal or demyelinating disease in c57bl/6 mice infected with theiler’s murine encephalomyelitis viruses
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864290/
https://www.ncbi.nlm.nih.gov/pubmed/35222374
http://dx.doi.org/10.3389/fimmu.2022.786940
work_keys_str_mv AT buhlermelanie ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT runftsandra ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT lidandan ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT gottingjasper ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT detjeclaudian ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT nippoldvanessa ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT stoffmelanie ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT beinekeandreas ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT schulzthomas ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT kalinkeulrich ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT baumgartnerwolfgang ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses
AT gerhauseringo ifnbdeficiencyresultsinfatalordemyelinatingdiseaseinc57bl6miceinfectedwiththeilersmurineencephalomyelitisviruses